A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3374911



Internal ID15221886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87331102..87331116hg38UCSC Ensembl
Innerchr9:87331093..87331125hg38UCSC Ensembl
Outerchr9:87331079..87331139hg38UCSC Ensembl
chr9:89946017..89946031hg19UCSC Ensembl
Innerchr9:89946008..89946040hg19UCSC Ensembl
Outerchr9:89945994..89946054hg19UCSC Ensembl
chr9:89135837..89135851hg18UCSC Ensembl
Innerchr9:89135860..89135828hg18UCSC Ensembl
Outerchr9:89135814..89135874hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8945315, essv8945318, essv8945323, essv8945325, essv8945321, essv8945314, essv8945330, essv8945317, essv8945320, essv8945326, essv8945332, essv8945309, essv8945311, essv8945319, essv8945328, essv8945331, essv8945334, essv8945308, essv8945306, essv8945338, essv8945316, essv8945337, essv8945329, essv8945310, essv8945339, essv8945322, essv8945307, essv8945305, essv8945312, essv8945327, essv8945333
SamplesNA18592, NA18959, NA19190, NA07357, NA18550, NA18519, NA18960, NA18916, NA18571, NA19138, NA18605, NA18871, NA18573, NA18499, NA18912, NA18853, NA18555, NA18523, NA18858, NA18593, NA18542, NA19108, NA18943, NA19093, NA18609, NA19102, NA18505, NA07000, NA18562, NA18965, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3374911
Frequency
Sample Size185
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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